Exome Sequencing Identifies a Novel MYH7 p.G407C Mutation Responsible for Familial Hypertrophic Cardiomyopathy

Hypertrophic cardiomyopathy (HCM), characterized by myocardial hypertrophy, is the most common cause of sudden cardiac arrest in young individuals. More than 270 mutations have been found to be responsible for familial HCM to date; mutations in MYH7, which encodes the β-myosin heavy chain (β-MHC) an...

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Detalhes bibliográficos
Main Authors: Guo, Qianqian, Xu, Yuejuan, Wang, Xike, Guo, Ying, Xu, Rang, Sun, Kun, Chen, Sun
Formato: Artigo
Idioma:Inglês
Publicado em: Mary Ann Liebert, Inc. 2014
Assuntos:
Protein Expression/Modification/Regulation
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4180301/
https://ncbi.nlm.nih.gov/pubmed/24963656
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1089/dna.2014.2483
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